L-Tetrahydropalmatine synergizes cytotoxic CD8+ T mediated antitumor and ferroptosis in gastric cancer

L-Tetrahydropalmatine (L-THP) is an isoquinoline alkaloid derived from the traditional Chinese herb Corydalis (genus Corydalis), particularly its analgesic and sedative effects. The in-depth function of L-THP on gastric cancer (GC) immune escape is still unclear. Here, the present research aimed to investigate the function of L-THP on GC antitumor response. Results indicated that L-THP promoted the cytotoxicity and antitumor response of CD8<sup>+</sup> T cells to GC cells. Moreover, L-THP up-regulated the ferroptosis of GC cells. Mechanistically, L-THP recognized the FSP1 protein and bound to FSP1 with high binding affinity. L-THP reduced the FSP1 stability to trigger the ferroptosis of GC cells. In conclusion, this study shows that L-THP synergizes cytotoxic CD8<sup>+</sup> T cell-mediated GC antitumor response and ferroptosis through FSP1, providing potent evidence for GC immunoregulation.

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Publication Details

Journal
Cell Death Discovery
Published
2025-11-24
DOI
https://doi.org/10.1038/s41420-025-02825-x
Citations
1
Primary Topic
Ferroptosis and cancer prognosis
Type
article
Field-Weighted Citation Impact
1.52
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article

L-Tetrahydropalmatine synergizes cytotoxic CD8+ T mediated antitumor and ferroptosis in gastric cancer

Yaqin Wei, Yu Lu, Le Zhou, Kai Lin
1 citations
Cell Death Discovery
Ferroptosis and cancer prognosis
1.52
article

L-Tetrahydropalmatine synergizes cytotoxic CD8+ T mediated antitumor and ferroptosis in gastric cancer

Yaqin Wei, Yu Lu, Le Zhou, Kai Lin
article en
1 citations

Abstract

L-Tetrahydropalmatine (L-THP) is an isoquinoline alkaloid derived from the traditional Chinese herb Corydalis (genus Corydalis), particularly its analgesic and sedative effects. The in-depth function of L-THP on gastric cancer (GC) immune escape is still unclear. Here, the present research aimed to investigate the function of L-THP on GC antitumor response. Results indicated that L-THP promoted the cytotoxicity and antitumor response of CD8<sup>+</sup> T cells to GC cells. Moreover, L-THP up-regulated the ferroptosis of GC cells. Mechanistically, L-THP recognized the FSP1 protein and bound to FSP1 with high binding affinity. L-THP reduced the FSP1 stability to trigger the ferroptosis of GC cells. In conclusion, this study shows that L-THP synergizes cytotoxic CD8<sup>+</sup> T cell-mediated GC antitumor response and ferroptosis through FSP1, providing potent evidence for GC immunoregulation.

Cell Death DiscoveryVol. 11(1)
University of Electronic Science and Technology of China (CN)
Openalex Percentile: Top 13%
Ferroptosis and cancer prognosis
1.52
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